identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
5810695D6FDE5B668DF5FB8B5BF07CD4.text	5810695D6FDE5B668DF5FB8B5BF07CD4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Eurycorypha paraspicula Hemp & Massa & Heller 2025	<div><p>Eurycorypha paraspicula sp. nov.</p><p>Material examined. —</p><p>Holotype: ♂; TANZANIA • East Usambara Mountains, Nilo Forest Reserve; 1500 m; montane forest; February 2021; CCH . Paratypes: 3 ♂; TANZANIA • same data as holotype; CCH • 1 ♂, same data as holotype; March 2021; CCH .</p><p>Description. —</p><p>Male. General habitus and color. A medium-sized species with a distinctly roundish appearance (Fig. 1 A, B). The tegmina display a pattern of white to yellowish veins on a dark green ground color. The rest of the body is speckled yellowish-green. In life, yellow fasciae are visible on the head and body. Head and antennae: Antennae thin, typical of Eurycorypha, reaching approximately to the tips of the flexed tegmina. Fastigium verticis about twice as wide as the scapus of the antenna; it meets the equally broad fastigium frontis along a well-developed horizontal line. The face bears callose carinae, yellow when alive. Eyes elongate and oval, typical for the genus. Thorax: Pronotal disc flat and smooth; anterior margin broadly incurved, posterior margin broadly rounded. Wings: Tegmina very roundish, about 2.3 times longer than broad; hind wings (alae) hardly visible. Legs: Fore coxa with a short, stout spine. Fore and mid femora dorsally unarmed; ventrally with 3–4 outer spines, lacking inner spines. Hind femora with 5–8 irregularly spaced spines near the apex on the ventral side. Fore and mid tibiae with a ventral double row of numerous spines. Hind tibiae with four rows of spines and three slender spurs on each side. Abdomen: Last abdominal tergite bearing two slender and sharply pointed spines at the posterior margin (Fig. 1 B, D). Cerci thick at the base, tapering toward rounded apices, each with a distinct sclerotized ridge (Fig. 1 C – E). Subgenital plate broad at the base, narrowing posteriorly; posterior margin incised, forming two short lateral processes; styli present (Fig. 1 E).</p><p>Female. — Unknown.</p><p>Measurements. —</p><p>(in mm) Males (n = 5) Total length: 30.3–31.8; body length: 18.2–22.7; pronotum length: 4.8–5.2; pronotum depth: 3.9–4.3; length of tegmina: 24–26.7; width of tegmina: 10.0–11.0; length of hind femur: 16.5–17.7.</p><p>Habitat and notes on biology. —</p><p>Montane forest at around 1500 m. a. s. l. Currently, this species has been collected only at the highest points of the East Usambara Mountains in the Nilo Forest Reserve. Despite regular visits to this area (19 times between 2012 and 2024), no females have been encountered. Similar to other montane Orthoptera species, it is likely present only during the warmer times of the year.</p><p>Distribution. —</p><p>Tanzania (East Usambara Mountains).</p><p>Diagnosis. —</p><p>Males of E. paraspicula are characterized by an unusually roundish habitus, which is uncommon within the genus. This species is morphologically most similar to E. spicula from the Nguru Mountains, but can be distinguished by the more rounded shape of the male body, longer paired spines on the posterior margin of the tenth abdominal tergite, and notably thicker cerci. The male cerci of E. paraspicula are robust and terminate in a distinct sclerotized ridge, whereas in E. spicula they are more slender with narrower tips. Most significantly, the acoustic signals of E. paraspicula differ from those of E. spicula, providing a reliable means of species recognition. The female of E. paraspicula is currently unknown.</p><p>Bioacoustics. —</p><p>The male song consists of groups of polysyllabic, crescendoing echemes (Figs 8 A, 9 A). An echeme contains 7.7 ± 0.5 syllables (4 males; 68 measurements; range 5–9), produced at an SRR of 41 Hz corresponding to a syllable period 24.4 ± 0.8 ms (range 20–28 ms; T = 24–25 ° C). One group of echemes typically contains 1.9 ± 0.3 elements (4 males; 35 measurements; range 1–3), repeated at periods of 1.56 ± 0.56 s (4 males; 37 measurements; range 1.2–2.4). These groups are separated by intervals of 8.7 ± 1.6 s (4 males; 32 measurements; range 4.6–24.2) from the next. The spectrum of the song shows a relatively narrow peak around 13 kHz (Fig. 11; see Table 1 for other details). Stridulatory file, tooth number, and tooth intervals are in the range typical for Eurycorypha (Table 1; for comparison, see Heller and Hemp 2020).</p><p>* from Heller and Hemp 2020; $ groups of syllables; pulse-like syllables; n. a. not available.</p></div>	https://treatment.plazi.org/id/5810695D6FDE5B668DF5FB8B5BF07CD4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Hemp, Claudia;Massa, Bruno;Heller, Klaus-Gerhard	Hemp, Claudia, Massa, Bruno, Heller, Klaus-Gerhard (2025): Description and bioacoustics of three new Eurycorypha (Orthoptera, Tettigonioidea) species from Tanzania and Ghana, with notes on their biology. Journal of Orthoptera Research 34 (2): 187-200, DOI: 10.3897/jor.34.137613
C01131A40F795CE3A73DAD7C5BC2E739.text	C01131A40F795CE3A73DAD7C5BC2E739.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Eurycorypha spicula Hemp & Massa & Heller 2025	<div><p>Eurycorypha spicula sp. nov.</p><p>Material examined. —</p><p>Holotype: TANZANIA • ♂; Nguru Mts; 1900 m a. s. l.; montane forest above Dibago / Maskati; November 2021; CCH . Paratypes: • 11 ♂, 11 ♀; same data as holotype; CCH .</p><p>Description. —</p><p>Male. Habitus and color. A roundish medium-sized species, green with lighter veins on the tegmina and speckled with white dots and patches on pronotum and head (Fig. 2 A). Color pattern white to yellowish veins on dark green background on the tegmina, rest of body also speckled yellowish-green. Head and antennae: Antennae typical of Eurycorypha, thin, about as long as flexed tegmina. Fastigium verticis about 2.4 times as wide as scapus of antenna; fastigium verticis meeting equally broad fastigium frontis along a well-developed horizontal line; face with callose frontogenal carinae, yellow when alive; eyes typical for Eurycorypha, elongate and oval. When alive, with yellow fasciae. Thorax: Pronotum with flat and smooth disc, anterior margin of pronotum broadly incurved, posterior margin broadly rounded. Wings: Tegmina roundish, only about 2.5 times longer than broad; alae only slightly protruding. Stridulatory file comparatively long, evenly curved, and about 2.2 mm long, consisting of very densely packed teeth. Legs: Fore coxa with very short, broad-based spine. Fore and mid femora dorsally unarmed, ventrally with 2–4 spines on outer side and without inner spines. Hind femora ventrally with 4 spines at apical end. Fore and mid tibiae with ventral double row of few spines (3–8). Hind tibiae with 4 rows of spines and three spurs at each side. Abdomen: Last abdominal tergite with two broad-based short spines at posterior margin (Fig. 3 A). Cerci thick at base, narrowing to their apices and ending in a sclerotized small ridge (Fig. 3 A, C, E). Subgenital plate with broad base. Posterior margin incised forming two short processes with small styli (Fig. 3 C).</p><p>Female. — Very roundish and compact, of same color pattern as male (Fig. 1 B). Ovipositor well-developed, upcurved (Fig. 3 B). Subgenital plate forming a triangular flap. Lateral margins of the lower valves are thickened, running in parallel to the subgenital plate and forming an ear-like grove or hole lateral at base of pronotum (Fig. 3 B, D, F).</p><p>Nymphs. — The first stages resemble black ants, gaining more color in stages two and three (Fig. 2 C, E). Unlike most other Eurycorypha species where nymphal stages are known, the nymphs of E. spicula are dorsally black on the head, the pronotum, and the abdomen, and the legs are partly black. The black coloration persists in the last two stages four and five (Fig. 2 F) and vanishes when molting to the adult, which is predominantly green (Fig. 2 A, B). Eight nymphs (L 1 – L 3) were collected in November 2024 at the same locality as in 2021, suggesting that this species hatches in November, coinciding with the onset of the short rains and rising temperatures.</p><p>Biology. —</p><p>L 1 and L 2 nymphs were collected in November 2021 from a flowering Bidens kilimanjari at an elevation of about 1900 m a. s. l. in the Nguru Mountains above Dibago / Maskati. They were taken to the laboratory and reared to adults on various leaves from trees and bushes at Mt Kilimanjaro. The first adults emerged on the 12 th of January 2022. Thus, as in most other Eurycorypha where development time from hatching to the adults is known, E. spicula takes about 2 months from hatching to the adult.</p><p>Some specimens were infected by Nematoida while reared in the lab. Fig. 4 shows a nematoid approximately 10 times the length of the insect that emerged from an adult female of E. spicula .</p><p>Measurements. —</p><p>(mm). Males (n = 13). Total length: 27.2–32.6; body length: 12.7–19.3; pronotum length: 4.1–4.6; pronotum depth: 3.1–3.5; length of tegmina: 20.8–27.1; width of tegmina: 9.2–10.6; length of hind femur: 13.4–15.2. Females (n = 9). Total length: 27.1–28.7; body length: 15.7–16.9; pronotum length: 4.2–4.8; pronotum depth: 3.2–3.7; length of tegmina: 22.7–24.6; width of tegmina: 9.5–11.5; length of hind femora: 13.9–16.6; ovipositor: 5.5–5.6.</p><p>Diagnosis. —</p><p>Males of E. spicula are somewhat roundish but less so than in the closely related E. paraspicula . They are distinguished by the presence of two relatively short spines at the posterior margin of the tenth abdominal tergite, and slender, tapering cerci with narrow tips that end in a small sclerotized point. Although morphologically very similar to E. paraspicula, the male of E. spicula can be differentiated by its more elongated appearance and less robust cerci. The female is known and displays a compact, roundish habitus, a well-developed upcurved ovipositor, and a triangular subgenital plate bordered by thickened ridges.</p><p>Bioacoustics. —</p><p>The male song consists of complicated and quite characteristic echemes. One relatively long syllable is followed by a series of shorter elements (Figs 8 B, 9 B). Surprisingly, some parameters of these echemes were quite variable in the three recorded males. The duration of the long syllables varied between 38.4 and 84.4 ms, the number of short syllables ranged between 6.8 and 11.8, and variation of the duration of the complete echeme was also not small (324–441 ms; all means of 3 males; n = 10 per male; T = 21 ° C). More constant were the periods between the beginning of the long syllable and that of the series of short syllables (138–152 ms) and between the short syllables (28.5–31 ms corresponding to 32–35 Hz SRR; measured from the beginning of the 5 th to that of the 6 th syllable). The echemes were repeated at intervals of several seconds. When two males were singing in acoustical contact, the structure of their echemes became more irregular (‘ leader’ in Fig. 10 A, B; upper line), while the other (‘ follower’ in Fig. 10; lower line) placed his echemes immediately after that of the first. Occasionally the leader also produced long series of short syllables.</p><p>The first answer of females was recorded approximately 417 ± 27 ms (mean ± SD; n = 10) after the beginning of the echeme, 281 ± 27 ms after the beginning of the syllable series, and 76.5 ± 30 ms after the end. However, in other situations (e. g., when several males were singing), the females responded more variable with latencies of the first response very close to the end of the male echeme (0.6 ± 50.1 ms – 2.6 ± 35.6 ms). The amplitude modulation of their response was also very variable, from single impulses (Fig. 9 B) to series of impulses, probably produced by repeated tegmen movements (Fig. 9 C). If they were not answers to their own songs, males reacted to these sounds, sometimes by producing a series of short syllables (Fig. 9 C). See the discussion for the function of the parts of the song.</p><p>The spectrum of the male song showed a broad peak around 13 kHz; that of the female was similar but even broader (Fig. 11; see Table 1 for other details). Male stridulatory file, tooth number, and inter-tooth intervals are in the range typical for Eurycorypha (Table 1; for comparison, see Heller and Hemp 2020).</p></div>	https://treatment.plazi.org/id/C01131A40F795CE3A73DAD7C5BC2E739	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Hemp, Claudia;Massa, Bruno;Heller, Klaus-Gerhard	Hemp, Claudia, Massa, Bruno, Heller, Klaus-Gerhard (2025): Description and bioacoustics of three new Eurycorypha (Orthoptera, Tettigonioidea) species from Tanzania and Ghana, with notes on their biology. Journal of Orthoptera Research 34 (2): 187-200, DOI: 10.3897/jor.34.137613
B56FACB0F4A15FA885F06D36DC47E0C3.text	B56FACB0F4A15FA885F06D36DC47E0C3.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Eurycorypha Stal 1873	<div><p>Genus Eurycorypha Stål, 1873</p><p>Type species. —</p><p>Phylloptera cereris Stål, 1873 .</p></div>	https://treatment.plazi.org/id/B56FACB0F4A15FA885F06D36DC47E0C3	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Hemp, Claudia;Massa, Bruno;Heller, Klaus-Gerhard	Hemp, Claudia, Massa, Bruno, Heller, Klaus-Gerhard (2025): Description and bioacoustics of three new Eurycorypha (Orthoptera, Tettigonioidea) species from Tanzania and Ghana, with notes on their biology. Journal of Orthoptera Research 34 (2): 187-200, DOI: 10.3897/jor.34.137613
1B7CFB9FA7AD5A86A2F77479409F3E08.text	1B7CFB9FA7AD5A86A2F77479409F3E08.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Eurycorypha willschi Hemp & Massa & Heller 2025	<div><p>Eurycorypha willschi sp. nov.</p><p>Material examined. —</p><p>Holotype: IVORY COAST • ♂; Comoé, Zamou; 10 Nov. 2014; light trap; leg. P. Moretto; MNHN . Paratypes: IVORY COAST • 1 ♂; same locality as holotype; 31 May 2016; light trap; leg. P. Moretto; MNHN • 2 ♂; same locality as holotype; 2 Nov. 2016; light trap; leg. P. Moretto; MNHN .</p><p>Additional material examined. —</p><p>IVORY COAST • 1 ♀; M’Banto; 6–8 Jul 2013; light trap; leg. P. Moretto; MNHN • 2 ♀; Comoé, Zamou; 2–10 Apr 2016; light trap; leg. P. Moretto; MNHN • 2 ♀; Comoé, Zamou; 19–22 Jun. 2017; light trap; leg. P. Moretto; MNHN • 1 ♀; Boudoukou, Zamou; Jul 2004; light trap; leg. P. Moretto; MNHN • 2 ♀; Kolomabira; 5 Jun 2016; light trap; leg. P. Moretto; MNHN • 1 ♀; Kolomabira; 2 Nov 2016; light trap; leg. P. Moretto; MNHN • 2 ♀; Mt. Tonkoui; 20 Jun 2015; light trap; leg. P. Moretto; MNHN • 2 ♀; Mt. Tonkoui; 17 Oct 2015; light trap; leg. P. Moretto; MNHN • 1 ♀; Mt. Tonkoui; 11 May 2017; light trap; leg. P. Moretto; BMPC • 1 ♀; Lamto, Toumodi, RBAP Bouhinta; 26 Jul 1962; MNHN • 1 ♀; Lamto; 15–16 Feb 1969; coll. C. Girard; MNHN • 9 ♂, 4 ♀; Lamto ( Toumodi); various dates: 20 Mar 1968, 15–30 Oct 1968, 15–21 Jan 1969, 1–12 Nov 1968, 20–30 Jul 1968, 14 Feb 1969, 15–25 Jul 1968, 15–30 Sep 1968, 24–31 Mar 1964, 24–31 Mar 1994, Nov 1966; coll. C. Girard; MNHN . • 1 ♀; Lamto (Toumodi), RBAP, Bauhinia; 25 Jul. 1952; coll. Paul Planquilte; MNHN . CENTRAL AFRICAN REPUBLIC • 1 ♂; La Maboké; Sep 1963; coll. R. Pujol; MNHN . NIGER • 1 ♂; Haut Niger et Benque; Ward 159-96; MNHN . BURKINA FASO • 1 ♂; Nazonga, Savane; 18–25 Oct 1986; coll. N. Berti &amp; Cl. Girard; MNHN . BURKINA FASO (Upper Volta) • 1 ♂; Bobo; 3 May 1966; coll. Gamontellgrie; MNHN . GUINEA • 1 ♂; Nimba; Dec 1956 – May 1957; leg. Lamotte, Amiet; coll. Vanderplaetsen; MNHN • 1 ♀; Nimba; Feb – Jun 1942; MNHN • 1 ♀; Kindia, Damakanya; 29–30 Jan 1951; coll. Bechyne; MNHN . BENIN (Dahomey) • 1 ♀; Ouidah; 1925; coll. Millet-Horsin; MNHN . NIGERIA • 1 ♂; Azare; Oct 1928; coll. Dr. Li Lloyd; NHM . CAMEROON • 1 ♀; Obout; 29 Jul – 12 Aug 2023; coll. A. Willsch . GHANA • 3 ♂, 5 ♀; Larabanga, near Mole National Park; 16–18 Oct 2022; coll. A. Willsch; CCH .</p><p>Description. —</p><p>Male. General habitus and color. A medium-sized, elongate species, predominantly green, with a faint pattern of white and yellowish, irregularly distributed veins on the tegmina. The head, pronotum, and body are green with whitish speckles, as observed in life (Fig. 5 A). When preserved, the white-yellowish pattern fades (Fig. 6 A). Head and antennae: Antennae typical of Eurycorypha, thin. Fastigium verticis approximately 2.2 times as wide as scapus of antenna; fastigium verticis meeting equally broad fastigium frontis along a well-developed horizontal line; face with evident frontogenal carinae; eyes typical for Eurycorypha, elongate and oval. Thorax: Pronotum with flat and smooth disc, anterior margin of pronotum broadly incurved, posterior margin rounded, lateral carinae evident. Wings: Tegmina elongate, rounded at tips, 3.5–3.8 times longer than broad. Legs. Fore femora dorsally unarmed, ventrally with 3–4 spines. Mid femora with 3 ventral outer spines. Hind femora with 5–7 ventral outer and inner spines. Fore tibiae with an open tympanum on both sides, with a ventral double row of 4–5 spines; mid tibiae with ventral double row of 4–6 spines. Hind tibiae with double row of 18–20 spines at ventral side; 3 slender sclerotized spurs at each side. Abdomen: Last abdominal tergite elongated like a stylus, formed by two parallel running parts; apex separated into two wing-like tips, the lateral sides expanded anteriorly to form two large tightly attached lobes (Fig. 6 B). From the underside, the two tips are nicely seen with a median oval part formed by the widened ventral margins of the structure that unite further anteriorly (Fig. 6 C). Cerci broad and laterally compressed with an inner lobe or dent midway; tips of cerci forming two wide lobes; the whole cercus strongly hairy. Subgenital plate of normal shape, broad at base and tapering to its apex; posterior margin broadly incised forming two short lateral processes; without styli (Fig. 6 C).</p><p>Female. — As the male, but with broader tegmina being 3.4–3.5 times longer than broad (Figs 5 B, 7 A). Ovipositor well-developed and strongly upcurved. The subgenital plate is a triangular flap with an almost rounded posterior margin, only slightly indented in middle. Gonangulum longish, ventrally bulbous. The margins of the lower valves form a thickened ridge within which the ventral bulbous part of the gonangulum is embedded.</p><p>Nymphs. — As seen in many Eurycorypha species with known nymphal stages, the first three stages of E. willschi resemble black ants. The nymphs gain more green color while growing and in stage 4 begin to lose their ant-like appearance, changing to leaf camouflage (in Fig. 5 C, three nymphal stages are seen together: L 1, L 2, and L 4). Eggs are oval and black and are laid singly into the margins of leaves (Fig. 5 D).</p><p>Measurements. —</p><p>(mm). Males (n = 4). Body length: 18.8–22.1; pronotum length: 4.3–4.8; pronotum depth: 3.9–4.2; length of tegmina: 27.1–28.1; width of tegmina: 7.2–8.0; length of hind femur: 13.5–14.5. Females (n = 8). Body length: 20.3–21.6; pronotum length: 4.3–5.0; pronotum depth: 4.3–4.8; length of tegmina: 29.3–32.1; width of tegmina: 8.4–9.2; length of hind femur: 15.0–16.5; length of ovipositor: 6.0–7.0.</p><p>Diagnosis. —</p><p>E. willschi, E. stylata Stål, 1873, and E. stenophthalma Chopard, 1963 are similar, differing in the males in the length of the stylus and the shape of the cerci (see images in OSF). They all have a distinct (but differently shaped) inner cercal tooth, missing in most Eurycorypha species (e. g., in all species known from East Africa). There are also new species belonging to this group of Eurycorypha species with a “ stylus-like ” 10 th abdominal tergite. These species will be treated in a revision of the genus currently in preparation.</p><p>The females of E. willschi have widened margins of the ventral valves of the ovipositor that form ear-like structures when viewed from above, as well as having bulbous parts of the ventral gonangulum (Fig. 7 B, C). Similar to E. willschi are the females of E. stenophthalma known from Chad that also have large bulbs beside the subgenital plate. The female of E. stylata is unknown. The male holotype of E. stylata was collected in Sierra Leone, and there are records also from Senegal (Hemp and Massa, in prep).</p><p>Etymology. —</p><p>E. willschi is named after Mr. Achim Willsch, collector of the life specimens of this species in Ghana.</p><p>Distribution. —</p><p>Widespread in West Africa.</p><p>Bioacoustics. —</p><p>In the male song, two different elements were observed. At first glance, both are quite similar (see Fig. 8), but they differ in SRR and function. Typically, several (to many) similar elements were repeated one after another. One of these elements invariably consists of pairs of syllables (Fig. 9 D; syllable period 34–38 ms; means of three males, n = 10–18 per male; SRR 26–29 Hz; T = 20–23 ° C). The period of the pairs — called slow echemes — is quite variable (period 4–28 s; means of three males, n = 10–11 per male; range of measurements 2.7–65 s; T = 20–23 ° C). These slow echemes could be heard for relatively long times (up to 10 minutes recorded). More typically, however, a male switched to a series of the other element after a shorter time. This element consisted of 2–3 syllables (Fig. 9 E; syllable period 20–22 ms; means of three males, n = 18–23 per male; T = 20–23 ° C), thus showing a clearly higher SRR (45–50 Hz); it is therefore called a fast echeme. Most of these series begin with elements of low amplitude and increase then in loudness (Fig. 11 C).</p><p>The females responded exclusively after these fast echemes. Their responses occurred 63–86 ms (means of three females, n = 10–12 per female; T = 20–23 ° C) after the beginning of the last (and loudest) syllable of the male echeme and 99–125 ms after the beginning of the first male syllable. Quite often the male added a series of very short syllables after the female’s response, occasionally even when the female had not answered. See discussion for the function of the parts of the song.</p><p>The spectrum of the male song showed a broad peak around 16.5 kHz; that of the female was similar but even broader (Fig. 11; see Table 1 for other details). Male stridulatory file, tooth number, and inter-tooth intervals are in the range typical for Eurycorypha (Table 1; for comparison, see Heller and Hemp 2020).</p><p>Spermatophore. —</p><p>During mating, the males transfer a spermatophore to the female as is typical for tettigonioids. At 51.5 mg (10 % male body mass), the size of the spermatophore is typical for the genus (see Table 2 for comparative data mainly based on specimens studied by Heller and Hemp 2020).</p></div>	https://treatment.plazi.org/id/1B7CFB9FA7AD5A86A2F77479409F3E08	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Hemp, Claudia;Massa, Bruno;Heller, Klaus-Gerhard	Hemp, Claudia, Massa, Bruno, Heller, Klaus-Gerhard (2025): Description and bioacoustics of three new Eurycorypha (Orthoptera, Tettigonioidea) species from Tanzania and Ghana, with notes on their biology. Journal of Orthoptera Research 34 (2): 187-200, DOI: 10.3897/jor.34.137613
